Effectiveness of Anti-Viral Medications for Treatment of Chronic Hepatitis C: A Retrospective Study in a Tertiary Care Hospital in Northeast Thailand

Authors

  • Bupachart Nunthaithaweekul Student, Master of Pharmacy Program in Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Khon Kaen University, Thailand
  • Tepsun Seearamroongruang Physician, Khon Kaen Hospital, Khon Kaen, Thailand
  • Manoon Mitpracha Physician, Khon Kaen Hospital, Khon Kaen, Thailand
  • Pornanan Domthong Physician, Khon Kaen Hospital, Khon Kaen, Thailand
  • Kittiya Piyasin Statistician, Khon Kaen Hospital, Khon Kaen, Thailand
  • Wilasinee Kamonmit Pharmacist, Khon Kaen Hospital, Khon Kaen, Thailand
  • Pissana Khonhome Pharmacist, Khon Kaen Hospital, Khon Kaen, Thailand
  • Guntaragorn Hongrattana Statistician, Khon Kaen Hospital, Khon Kaen, Thailand
  • Acharawan Topark-ngarm Assistant Professor, Division of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Khon Kaen University, Thailand

Keywords:

Hepatitis C virus infection, anti-viral medications, Sustained Virologic Response

Abstract

The objectives of the study were to assess the effectiveness of the anti-viral medications for treatment of chronic hepatitis C virus (HCV) infection and the factors associated with the effectiveness. The method was a retrospective study conducted in outpatients treated with anti-HCV medications at Khon Kaen hospital during January 1st 2019 to December 31st 2020. Demographic, social history, and medical history data were collected from medical records. Effectiveness was determined as an undetectable HCV RNA in the blood (<25 IU/mL) at 12 weeks post-treatment (Sustained Virologic Response; SVR12) and analyzed using descriptive analysis. Multivariate logistic regression analysis was used to identify factors associated with the effectiveness. The results showed that from a total of 160 patients included to the study, HCV genotypes 1, 3, 6 were found in 38.8, 43.1, and 18.1%, respectively. Majority of the patients were male (76.2%) and the average age was 50.5years. There were 75 patients (46.9%) having cirrhosis, 16 (10.0%) having HIV infection, and 22 (13.8%) having a previous treatment failure. Overall, SVR12 was achieved in 153 patients (95.6%). The SVR12 rate of genotype 3 was 98.6%.  Patients with HCV genotype 1 achieved SVR12 at 95.7% in non-cirrhosis group and 94.9% in cirrhosis group. Similarly, SVR12 of genotype 6 patients was achieved in 100% and 84.2% in non-cirrhosis and cirrhosis group, respectively. Three significant factors, including female gender (adjusted odds ratio (OR) 0.11; 95% CI 0.02-0.85), co-infection with HIV (OR 0.06; 95% CI 0.01-0.53) and genotype 6 with cirrhosis (OR 0.04; 95% CI 0.01-0.45), were negatively associated with treatment effectiveness. In conclusions, anti-HCV treatment was effective for genotype 1, 3, and 6 infections. The patients with no cirrhosis were likely to have better respond to the anti-HCV treatment. Female gender, co-infection with HIV, and genotype 6 with cirrhosis were significant factors negatively affecting effectiveness of HCV treatment.

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Published

2024-08-01

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บทความวิจัย